Hyperhaemolysis in a pregnant woman with a homozygous β 0 ‐thalassemia mutation and two genetic modifiers-Reference-Cited by-同舟云学术

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Hyperhaemolysis in a pregnant woman with a homozygous β 0 ‐thalassemia mutation and two genetic modifiers

Published:2021-05-07 Issue:7 Volume:9 Page:
ISSN:2324-9269
Container-title:Molecular Genetics & Genomic Medicine
language:en
Short-container-title:Mol Genet Genomic Med

Author:

Jiwu Lou¹^ORCID,Manna Sun²,Lai Meixiang³,Ying Zhao¹,Yanhui Liu¹

Affiliation:

1. Prenatal Diagnostic Center Dongguan Maternal & Children Health Hospital Dongguan China

2. Department of Obstetrics & Gynecology Dongguan Maternal and Children Hospital Dongguan China

3. Department of Obstetrics & Gynecology Dongguan Gaobu Hospital Dongguan China

Publisher

Wiley

Subject

Genetics (clinical),Genetics,Molecular Biology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/mgg3.1696

Reference14 articles.

1. A Genetic Variant Ameliorates β-Thalassemia Severity by Epigenetic-Mediated Elevation of Human Fetal Hemoglobin Expression

2. Hyperhemolysis in Patients With Hemoglobinopathies: A Single-Center Experience and Review of the Literature

3. A novel mutation in the erythroid transcription factor KLF1 is likely responsible for ameliorating β‐thalassemia major

4. A 3-bp deletion in the HBS1L-MYB intergenic region on chromosome 6q23 is associated with HbF expression

5. Genetic Variants Within the Erythroid Transcription Factor, KLF1, and Reduction of the Expression of Lutheran and Other Blood Group Antigens: Review of the In(Lu) Phenotype

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1. Single Nucleotide Polymorphisms in XMN1-HBG2, HBS1L-MYB, and BCL11A and Their Relation to High Fetal Hemoglobin Levels That Alleviate Anemia;Diagnostics;2022-06-02

2. Methylprednisolone;Reactions Weekly;2022-03

3. More than sample providers: how genetic researchers in Pakistan mobilized a prenatal diagnostic service for thalassemia;BioSocieties;2021-11-22

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